Anderson G P, Sanderson D G, Lee C H, Durell S, Anderson L B, Gross E L
Department of Biochemistry, Ohio State University, Columbus 43210-1292.
Biochim Biophys Acta. 1987 Dec 17;894(3):386-98. doi: 10.1016/0005-2728(87)90117-4.
Chemical modification of plastocyanin was carried out using ethylenediamine plus a water-soluble carbodiimide, which has the effect of replacing a negatively charged carboxylate group with a positively charged amino group at pH 6-8. The conditions were adjusted to produce a series of singly and doubly modified forms of plastocyanin. Differences in charge configuration allowed separation of these forms on a Pharmacia fast protein liquid chromatograph using a Mono Q anion exchange column. These forms were used to study the interaction of plastocyanin with its reaction partner cytochrome f. The rate of cytochrome f oxidation was progressively inhibited upon incorporation of increasing numbers of ethylenediamine moieties indicating a positively charged binding site on cytochrome f. However, differential inhibition was obtained for the various singly modified forms allowing mapping of the binding site on plastocyanin. The greatest inhibition was found for forms modified at negatively charged residues Nos. 42-45 and Nos. 59-61 which comprise a negative patch surrounding Tyr-83. In contrast, the form modified at residue No. 68, on the opposite side of the globular plastocyanin molecule, showed the least inhibition. It can be concluded that the binding site for cytochrome f is located in the vicinity of residues Nos. 42-45 and Nos. 59-61. Modification of plastocyanin at residues Nos. 42-45 showed no effect on the rate of P-700+ reduction, suggesting that these residues are not involved in the binding of Photosystem I. However, an increase in the rate of P-700+ reduction was observed for plastocyanins modified at residue No. 68 or Nos. 59-61, which is consistent with the idea that the reaction domain of Photosystem I is negatively charged and Photosystem I binds at the top of the molecule and accepts electrons via His-87 in plastocyanin. These results raise the possibility that plastocyanin can bind both cytochrome f and Photosystem I simultaneously. The effect of ethylenediamine modification on the formal potential of plastocyanin was also examined. The formal potential of control plastocyanin was found to be +372 +/- 5 mV vs. normal hydrogen electrode at pH 7. All modified forms showed a positive shift in formal potential. Singly modified forms showed increases in formal potentials between +8 and +18 mV with the largest increases being observed for plastocyanins modified at residues Nos. 42-45 or Nos. 59-61.
使用乙二胺和水溶性碳二亚胺对质体蓝素进行化学修饰,其作用是在pH 6 - 8的条件下,用带正电荷的氨基取代带负电荷的羧基。调整条件以产生一系列单修饰和双修饰形式的质体蓝素。电荷构型的差异使得这些形式能够在Pharmacia快速蛋白质液相色谱仪上使用Mono Q阴离子交换柱进行分离。这些形式用于研究质体蓝素与其反应伙伴细胞色素f的相互作用。随着乙二胺基团数量的增加,细胞色素f的氧化速率逐渐受到抑制,这表明细胞色素f上存在一个带正电荷的结合位点。然而,对于各种单修饰形式获得了差异抑制,从而能够绘制质体蓝素上的结合位点。在带负电荷的第42 - 45位残基和第59 - 61位残基处修饰的形式抑制作用最大,这些残基构成了围绕Tyr - 83的负电斑块。相反,在球状质体蓝素分子另一侧的第68位残基处修饰的形式显示出最小的抑制作用。可以得出结论,细胞色素f的结合位点位于第42 - 45位残基和第59 - 61位残基附近。在第42 - 45位残基处修饰质体蓝素对P - 700 +还原速率没有影响,这表明这些残基不参与光系统I的结合。然而,在第68位残基或第59 - 61位残基处修饰的质体蓝素观察到P - 700 +还原速率增加,这与光系统I的反应域带负电荷且光系统I在分子顶部结合并通过质体蓝素中的His - 87接受电子的观点一致。这些结果增加了质体蓝素可以同时结合细胞色素f和光系统I的可能性。还研究了乙二胺修饰对质体蓝素形式电位的影响。在pH 7时,对照质体蓝素的形式电位相对于标准氢电极测得为+372 +/- 5 mV。所有修饰形式的形式电位都出现正移。单修饰形式的形式电位增加了+8至+18 mV,在第42 - 45位残基或第59 - 61位残基处修饰的质体蓝素增加幅度最大。